APA (7th ed.) Citation

Elsayed, S. M., Heller, R., Thoenes, M., Zaki, M. S., Swan, D., Elsobky, E., . . . Bolz, H. J. (2014). Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. European Journal of Human Genetics, 22(2), 286. https://doi.org/10.1038/ejhg.2013.150

Chicago Style (17th ed.) Citation

Elsayed, Solaf M., et al. "Autosomal Dominant SCA5 and Autosomal Recessive Infantile SCA Are Allelic Conditions Resulting from SPTBN2 Mutations." European Journal of Human Genetics 22, no. 2 (2014): 286. https://doi.org/10.1038/ejhg.2013.150.

MLA (9th ed.) Citation

Elsayed, Solaf M., et al. "Autosomal Dominant SCA5 and Autosomal Recessive Infantile SCA Are Allelic Conditions Resulting from SPTBN2 Mutations." European Journal of Human Genetics, vol. 22, no. 2, 2014, p. 286, https://doi.org/10.1038/ejhg.2013.150.